QA Inspector Bilingual EnglishSpanish

5TH HQ; Fort Lauderdale (FL); On-site; USD 51,577,344 - 68,769,792; Full time

Job summary

5TH HQ is seeking a bilingual QA Inspector in Davie, FL to join a cGMP manufacturing environment. The role emphasizes attention to detail, documentation accuracy, and regulatory compliance, with a shift schedule from early morning to early afternoon.

The position is full-time with temp-to-hire potential. The ideal candidate has 1–3 years QA/QC experience, familiarity with GDP, cGMP, and FDA regulations, and the ability to operate pallet jacks.

Qualifications

• Associate degree or equivalent work experience.
• 1–3 years of QA/QC in a manufacturing environment.
• Previous warehouse experience preferred.
• Bilingual English/Spanish required.
• Knowledge of cGMP regulations and FDA guidelines.
• Detail-oriented with strong documentation skills.
• Basic computer and math skills.

Responsibilities

• Inspect in-process products and complete documentation.
• Ensure cGMP compliance on the production floor.
• Perform QA tasks, sampling, inspections, and testing per SOPs and FDA/DEA regs.
• Document work activities in batch records and logs.
• Inform management of deviations from standards.
• Inspect rooms, lines, and equipment prior to use.
• Review records for GDP and cGMP compliance.
• Apply disposition status to components and materials.
• Issue QA alerts when issues are identified.
• Perform other duties as assigned by supervisor.

Skills

Bilingual English/Spanish

Detail oriented

Quality Assurance

cGMP knowledge

Documentation

Data entry

Math skills

Education

Associate degree

Tools

Pallet jack

Job description

We're currently seeking a bilingual QA Inspector for one of our clients in Davie, FL. This is an excellent opportunity for a detail-oriented quality professional with experience in a cGMP manufacturing environment who is looking to join a growing organization committed to quality, safety, and regulatory compliance.

Location: Davie, FL
Schedule: Monday–Friday, 5:30 AM – 2:00 PM (1st Shift)
Employment Type: Full-Time, Temp-to-Hire

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES

• Responsible for performing inspections of in-process products and completing the appropriate documentation.
• Ensure cGMP compliance at all times on the production floor.
• Perform Quality Assurance tasks such as sampling, inspections, and testing to ensure manufactured products comply with internal SOPs, safety initiatives, company policies, and FDA and DEA regulations.
• Document all work performed, ensuring accuracy and completeness.
• Inform management of any deviations from established standards or procedures.
• Inspect and approve rooms, production lines, and equipment prior to use by Manufacturing and R&D personnel.
• Approve components for in-process operations.
• Monitor manufacturing and packaging areas for compliance with internal SOPs, cGMP regulations, and FDA/DEA requirements.
• Document all work activities in batch records, forms, and logs to ensure accuracy and compliance.
• Sample in-process materials and finished products. Perform required inspections and testing, then process and distribute samples to the appropriate departments.
• Review records for cGMP compliance, accuracy, completeness, and Good Documentation Practices (GDP).
• Inform management of problems, failures, and deviations from internal and regulatory standards.
• Apply disposition status to components and in-process materials.
• Issue QA Alerts whenever questionable components, in-process materials, or finished products are identified during production or storage.
• Perform other duties as assigned by the immediate supervisor.

QUALIFICATIONS

• Associate degree or equivalent work experience.
• 1–3 years of Quality Assurance or Quality Control experience in a manufacturing environment.
• Previous warehouse experience preferred.
• Experience operating a manual or electric pallet jack preferred.
• Bilingual (English/Spanish) required.
• Knowledge of cGMP regulations and FDA guidelines.
• Detail-oriented.
• Basic computer and math skills.

PHYSICAL REQUIREMENTS

Requires standing, walking, bending, lifting, and handling chemicals, as well as using computers and monitoring equipment. Must be able to lift and carry boxes weighing up to 50 pounds on a regular basis. Must be able to wear appropriate PPE, including face masks, respirators, safety goggles, and hearing protection.

TYPICAL WORK CONDITIONS

Subject to exposure to food and nutritional bulk ingredients that may affect the respiratory system or skin, including odors, dust, and airborne allergens.

Works in a dry, low-moisture manufacturing environment with exposure to normal workplace hazards, including proximity to moving mechanical parts and moderate industrial noise.